rs6699417
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6699417(C;C) |
Make rs6699417(C;T) |
Make rs6699417(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 88657760 |
Gene | PKN2-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs6699417 |
dbSNP (classic) | rs6699417 |
ClinGen | rs6699417 |
ebi | rs6699417 |
HLI | rs6699417 |
Exac | rs6699417 |
Gnomad | rs6699417 |
Varsome | rs6699417 |
LitVar | rs6699417 |
Map | rs6699417 |
PheGenI | rs6699417 |
Biobank | rs6699417 |
1000 genomes | rs6699417 |
hgdp | rs6699417 |
ensembl | rs6699417 |
geneview | rs6699417 |
scholar | rs6699417 |
rs6699417 | |
pharmgkb | rs6699417 |
gwascentral | rs6699417 |
openSNP | rs6699417 |
23andMe | rs6699417 |
SNPshot | rs6699417 |
SNPdbe | rs6699417 |
MSV3d | rs6699417 |
GWAS Ctlg | rs6699417 |
GMAF | 0.3889 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20881960] |
Trait | |
Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
Risk Allele | T |
P-val | 5E-9 |
Odds Ratio | 0.0200 [NR] meters increase |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 1
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d